US20020128154A1 - Continous process for the preparation of a stable herbicidal aqueous suspension concentrate composition - Google Patents

Continous process for the preparation of a stable herbicidal aqueous suspension concentrate composition Download PDF

Info

Publication number
US20020128154A1
US20020128154A1 US09/938,371 US93837101A US2002128154A1 US 20020128154 A1 US20020128154 A1 US 20020128154A1 US 93837101 A US93837101 A US 93837101A US 2002128154 A1 US2002128154 A1 US 2002128154A1
Authority
US
United States
Prior art keywords
process according
mixture
group
pendimethalin
suspension concentrate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US09/938,371
Other versions
US6617280B2 (en
Inventor
Jean-Paul Fafchamps
Jean-Michel Villanueva
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Priority to US09/938,371 priority Critical patent/US6617280B2/en
Assigned to BASF AKTIENGESELLSCHAFT reassignment BASF AKTIENGESELLSCHAFT ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: VILLANUEVA, JEAN-MICHEL, FAFCHAMPS, JEAN-PAUL
Publication of US20020128154A1 publication Critical patent/US20020128154A1/en
Application granted granted Critical
Publication of US6617280B2 publication Critical patent/US6617280B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N33/00Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/02Amines; Quaternary ammonium compounds
    • A01N33/12Quaternary ammonium compounds
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N33/00Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/16Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
    • A01N33/18Nitro compounds

Definitions

  • Stable aqueous suspension concentrate compositions of pendimethalin, alone or in combination with a secondary herbicide, and methods for their preparation are described in U.S. Pat. No. 5,624,884.
  • the methods so described are 2-step methods wherein the first step is the formation of a hot aqueous emulsion of molten pendimethalin and the second step is the cooling of said emulsion to crystallize the pendimethalin and form an aqueous suspension concentrate.
  • a third milling step may be added.
  • the discreet steps of forming a hot emulsion, then cooling said emulsion and optionally milling said cooled emulsion entail a non-integrated batch procedure. That is the desired product must be produced in discreet batches of a fixed quantity and the process must begin, end and start again, repeatedly.
  • Such batch processes, when producing quantities on a manufacturing scale can be time-consuming, and labor and energy intensive.
  • said stable herbicidal compositions may be prepared efficently and effectively with reduced time, labor and energy resources.
  • the present invention provides a process for the preparation of an aqueous suspension concentrate composition which comprises mixing a molten pendimethalin stream having a temperature of about 57° to 75° C. with an aqueous stream containing coformulants plus seed crystals of orange pendimethalin said aqueous stream having a temperature of about ⁇ 3° C. to 5° C.
  • Pendimethalin is a low-melting dinitroaniline herbicide useful in agricultural, horticultural and turf applications.
  • pendimethalin exists primarily in two polymorphic forms, generally referred to as the orange form and the yellow form. It is known that compositions containing crystalline pendimethalin in 100% of the orange form or in a ratio of 96:4 of the orange form to the yellow form demonstrate enhanced stability.
  • control of the poylmorph ratio of pendimethalin in a process involving the conversion of molten pendimethalin to solid pendimethalin is known to be difficult.
  • U.S. Pat. No. 5,624,884 describes stable aqueous suspension concentrate compositions of pendimethalin and methods for their preparation. However, said methods require a two-step procedure which necessitates a batch production effort.
  • a stable aqueous suspension concentrate composition of pendimethalin may be prepared in a continuous single-step procedure which comprises the high shear mixing of a molten pendimethalin stream, having a temperature of about 57° to 75° C., with an aqueous stream containing coformulants plus seed crystals of orange pendimethalin, said aqueous stream having a temperature of about ⁇ 3° C. to 5° C.
  • the process of the invention instantaneously and continuously generates a cool stable aqueous suspension of fine, regular, orange crystals of pendimethalin.
  • the process of the invention may be run continuously by any conventional means such as an in-line high shear disperser/homogenizer. Alternatively, the process may be run in batch fashion, if so desired.
  • the stable herbicidal aqueous suspension concentrate composition produced by the process of the invention may optionally be milled to obtain an average particle size of suspended particles of less than 5-20 microns.
  • the process of the invention may also be used to prepare stable aqueous suspension concentrate compositions containing pendimethalin in combination with one or more pesticides which are low-melting or water-soluble.
  • one or more pesticides which are low-melting or water-soluble.
  • an additional water-soluble pesticide may be included in the cooled aqueous stream, prior to the mixing of the two streams.
  • Compositions produced by the process of the invention typically comprise on a weight to volume basis, about 5.0% to 50.0% pendimethalin; about 0% to 50.0% of one or more additional pesticides which are water soluble; about 3.0% to 30.0% of coformulants, such as surfactants, dispersing agents, wetting agents, antifreeze agents, antifoam agents, suspending agents, thickeners, preservatives or the like; and about 20.0% to 92.0% water.
  • coformulants such as surfactants, dispersing agents, wetting agents, antifreeze agents, antifoam agents, suspending agents, thickeners, preservatives or the like.
  • coformulant designates an ingredient such as: a water-soluble pesticide, i.e. a herbicide, fungicide, insecticide, plant growth regulant, or the like; an antifreeze agent, i.e. ethylene glycol, propylene glycol, glycerine, urea, or the like; an antifoam agent, i.e. silicon, or the like; a suspending agent, i.e. silica, MgSO 4 , or the like; a thickener, i.e. clay, polyvinyl alcohol, polyvinylpyrrolidone, polyacrylamide, or the like; a preservative, i.e.
  • a water-soluble pesticide i.e. a herbicide, fungicide, insecticide, plant growth regulant, or the like
  • an antifreeze agent i.e. ethylene glycol, propylene glycol, glycerine, urea, or the like
  • an antifoam agent i
  • Water-soluble pesticides contemplated for use in the process of the invention include herbicides, for example: quaternary salts of amino phosphonic or phosphinic acids such as glyphosate, glufosinate, or the like; substituted phenoxy or benzoic acid salts such as 2,4-D, 2,4-DB, MCPP, MCPA, dicamba, chloramben, or the like; imidazolinones such as imazaquin, imazethapyr, imazamox, imazapic, imazapyr, or the like; or any of the known water-soluble herbicidal agents which possess physical/chemical properties known to be amenable to the preparation of aqueous suspension concentrate compositions. Fungicides, insecticides or plant growth regulants which are water-soluble and possess physical/chemical properties which are amenable to the preparation of aqueous suspension concentrate compositions are also contemplated.
  • herbicides for example: quaternary salts of amino phosphonic or
  • Surfactants suitable for use as a coformulant in the process of the invention include: ethylene oxide/propylene oxide condensates; alkylaryl- or arylarylethoxylates or derivatives thereof; lignosulfonates; cresol- or naphthalene-formaldehyde condensates or the sulfonates thereof; polycarboxylates or derivatives thereof; or mixtures thereof.
  • Preferred surfactants are: anionic polymerics, such as mixtures of alkylaryl- or arylarylethoxylates or their derivatives; cresol formaldehyde condensates or their sulfonates; naphthalene formaldehyde condensates or their sulfonates; or lignosulfonates. More preferred surfactants are mixtures of alkyl, aryl- and arylarylethoxylates or their derivatives.
  • stable aqueous suspension concentrate compositions of pendimethalin may be prepared by high-shear mixing of a stream of molten pendimethalin having a temperature of about 57° to 75° C. with an aqueous stream containing co-formulants plus orange pendimethalin seed crystals said aqueous stream having a temperature of about ⁇ 3° to 5° C.
  • the process of the invention facilitates optimum production with significantly increased conservation of time, labor and energy resources.
  • the thus-produced suspension concentrate may be bead-milled at 20-29° C. to achieve a particle size of less than 5-20 microns.
  • Water-soluble pesticides may be co-formulated with pendimethalin using the process of the invention by dissolving said pesticide in the aqueous stream containing coformulants plus orange pendimethalin seed crystals prior to mixing with the molten pendimethalin stream.
  • compositions produced by the process of the invention do not form large, elongated crystals after being processed. Therefore, processing and manufacturing is not halted because of aggregation due to crystal growth. Further, the agronomic application and efficacy of the suspension concentrate product is not hampered nor compromised by uneven particle size, sedimentation, or crystal growth.
  • An aqueous stream containing coformulants and 16-24% of orange crystalline pendimethalin is pre-cooled to temperatures of -3° C. to 5° C. and mixed in a high-shear disperser/homogenizer with a stream of molten pendimethalin at temperatures of 57° C. to 75° C. to yield a concentrated aqueous suspension of orange crystalline pendimethalin.

Abstract

The present invention provides a continuous process for the preparation of a stable aqueous suspension concentrate composition of pendimethalin, alone or in combination with another pesticide, which comprises mixing a molten stream of pendimethalin with a cold aqueous stream containing coformulants plus seed crystals of orange pendimethalin.

Description

    BACKGROUND OF THE INVENTION
  • Stable aqueous suspension concentrate compositions of pendimethalin, alone or in combination with a secondary herbicide, and methods for their preparation are described in U.S. Pat. No. 5,624,884. However, the methods so described are 2-step methods wherein the first step is the formation of a hot aqueous emulsion of molten pendimethalin and the second step is the cooling of said emulsion to crystallize the pendimethalin and form an aqueous suspension concentrate. Optionally, a third milling step may be added. The discreet steps of forming a hot emulsion, then cooling said emulsion and optionally milling said cooled emulsion, entail a non-integrated batch procedure. That is the desired product must be produced in discreet batches of a fixed quantity and the process must begin, end and start again, repeatedly. Such batch processes, when producing quantities on a manufacturing scale can be time-consuming, and labor and energy intensive. [0001]
  • Therefore, it is an object of this invention to provide a single-step continuous process suitable for the preparation of a stable herbicidal aqueous suspension concentrate composition on a manufacturing scale. [0002]
  • It is an advantage of this invention that said stable herbicidal compositions may be prepared efficently and effectively with reduced time, labor and energy resources. [0003]
  • SUMMARY OF THE INVENTION
  • The present invention provides a process for the preparation of an aqueous suspension concentrate composition which comprises mixing a molten pendimethalin stream having a temperature of about 57° [0004] to 75° C. with an aqueous stream containing coformulants plus seed crystals of orange pendimethalin said aqueous stream having a temperature of about −3° C. to 5° C.
  • DETAILED DESCRIPTION OF THE INVENTION
  • Pendimethalin is a low-melting dinitroaniline herbicide useful in agricultural, horticultural and turf applications. In its solid form, pendimethalin exists primarily in two polymorphic forms, generally referred to as the orange form and the yellow form. It is known that compositions containing crystalline pendimethalin in 100% of the orange form or in a ratio of 96:4 of the orange form to the yellow form demonstrate enhanced stability. However, control of the poylmorph ratio of pendimethalin in a process involving the conversion of molten pendimethalin to solid pendimethalin is known to be difficult. U.S. Pat. No. 5,624,884 describes stable aqueous suspension concentrate compositions of pendimethalin and methods for their preparation. However, said methods require a two-step procedure which necessitates a batch production effort. [0005]
  • Surprisingly it has now been found that a stable aqueous suspension concentrate composition of pendimethalin may be prepared in a continuous single-step procedure which comprises the high shear mixing of a molten pendimethalin stream, having a temperature of about 57° to 75° C., with an aqueous stream containing coformulants plus seed crystals of orange pendimethalin, said aqueous stream having a temperature of about −3° C. to 5° C. Advantageously, the process of the invention instantaneously and continuously generates a cool stable aqueous suspension of fine, regular, orange crystals of pendimethalin. The process of the invention may be run continuously by any conventional means such as an in-line high shear disperser/homogenizer. Alternatively, the process may be run in batch fashion, if so desired. The stable herbicidal aqueous suspension concentrate composition produced by the process of the invention may optionally be milled to obtain an average particle size of suspended particles of less than 5-20 microns. [0006]
  • The process of the invention may also be used to prepare stable aqueous suspension concentrate compositions containing pendimethalin in combination with one or more pesticides which are low-melting or water-soluble. For example, an additional water-soluble pesticide may be included in the cooled aqueous stream, prior to the mixing of the two streams. [0007]
  • Compositions produced by the process of the invention typically comprise on a weight to volume basis, about 5.0% to 50.0% pendimethalin; about 0% to 50.0% of one or more additional pesticides which are water soluble; about 3.0% to 30.0% of coformulants, such as surfactants, dispersing agents, wetting agents, antifreeze agents, antifoam agents, suspending agents, thickeners, preservatives or the like; and about 20.0% to 92.0% water. [0008]
  • As used in the specification and claims, the term coformulant designates an ingredient such as: a water-soluble pesticide, i.e. a herbicide, fungicide, insecticide, plant growth regulant, or the like; an antifreeze agent, i.e. ethylene glycol, propylene glycol, glycerine, urea, or the like; an antifoam agent, i.e. silicon, or the like; a suspending agent, i.e. silica, MgSO[0009] 4, or the like; a thickener, i.e. clay, polyvinyl alcohol, polyvinylpyrrolidone, polyacrylamide, or the like; a preservative, i.e. formaldehyde, methyl or propyl parahydroxybenzoate, sodium benzoate, or the like; a surfactant such as a dispersing agent, a wetting agent or the like; or any standard inert ingredient conventionally used in agricultural suspension concentrate compositions.
  • Water-soluble pesticides contemplated for use in the process of the invention include herbicides, for example: quaternary salts of amino phosphonic or phosphinic acids such as glyphosate, glufosinate, or the like; substituted phenoxy or benzoic acid salts such as 2,4-D, 2,4-DB, MCPP, MCPA, dicamba, chloramben, or the like; imidazolinones such as imazaquin, imazethapyr, imazamox, imazapic, imazapyr, or the like; or any of the known water-soluble herbicidal agents which possess physical/chemical properties known to be amenable to the preparation of aqueous suspension concentrate compositions. Fungicides, insecticides or plant growth regulants which are water-soluble and possess physical/chemical properties which are amenable to the preparation of aqueous suspension concentrate compositions are also contemplated. [0010]
  • Surfactants (including dispersing agents and wetting agents) suitable for use as a coformulant in the process of the invention include: ethylene oxide/propylene oxide condensates; alkylaryl- or arylarylethoxylates or derivatives thereof; lignosulfonates; cresol- or naphthalene-formaldehyde condensates or the sulfonates thereof; polycarboxylates or derivatives thereof; or mixtures thereof. Preferred surfactants are: anionic polymerics, such as mixtures of alkylaryl- or arylarylethoxylates or their derivatives; cresol formaldehyde condensates or their sulfonates; naphthalene formaldehyde condensates or their sulfonates; or lignosulfonates. More preferred surfactants are mixtures of alkyl, aryl- and arylarylethoxylates or their derivatives. [0011]
  • Accordingly, stable aqueous suspension concentrate compositions of pendimethalin may be prepared by high-shear mixing of a stream of molten pendimethalin having a temperature of about 57° to 75° C. with an aqueous stream containing co-formulants plus orange pendimethalin seed crystals said aqueous stream having a temperature of about −3° to 5° C. In actual practice, a molten stream of technical pendimethalin at 57° to 75° C. is continuously fed into a high-shear disperser/homogenizer simultaneously with an aqueous stream containing coformulants and about 16-24% of orange pendimethalin seed crystals, the aqueous stream having been pre-cooled to temperatures of about −3° C. to 5° C. to produce a continuous exit stream of a stable aqueous suspension concentrate composition of pendimethalin. By continuously, simultaneously feeding and mixing the molten pendimethalin and cooled aqueous streams in an in-line disperser/homogenizer while continuously discharging the resulting orange suspension concentrate composition, the process of the invention facilitates optimum production with significantly increased conservation of time, labor and energy resources. Optionally, the thus-produced suspension concentrate may be bead-milled at 20-29° C. to achieve a particle size of less than 5-20 microns. [0012]
  • Water-soluble pesticides may be co-formulated with pendimethalin using the process of the invention by dissolving said pesticide in the aqueous stream containing coformulants plus orange pendimethalin seed crystals prior to mixing with the molten pendimethalin stream. [0013]
  • Beneficially, compositions produced by the process of the invention do not form large, elongated crystals after being processed. Therefore, processing and manufacturing is not halted because of aggregation due to crystal growth. Further, the agronomic application and efficacy of the suspension concentrate product is not hampered nor compromised by uneven particle size, sedimentation, or crystal growth. [0014]
  • For a more clear understanding of the invention, the following examples are set forth below. These examples are merely illustrative and are not understood to limit the scope or underlying principles of the invention in any way. Indeed, various modifications of theinvention, in addition to those shown and describedgerein, will become apparent to those skilled in the art from the following examples and the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. [0015]
  • Unless otherwise noted, all parts are parts by weight. [0016]
  • EXAMPLES 1-7 Preparation of Stable Aqueous Suspension Concentrate Compositions of Pendimethalin
  • An aqueous stream containing coformulants and 16-24% of orange crystalline pendimethalin is pre-cooled to temperatures of -3° C. to 5° C. and mixed in a high-shear disperser/homogenizer with a stream of molten pendimethalin at temperatures of 57° C. to 75° C. to yield a concentrated aqueous suspension of orange crystalline pendimethalin. [0017]
  • Using the above procedure, the aqueous suspension concentrate compositions shown on Table I are obtained. [0018]
    TABLE I
    1 2 3 4 5 6 7
    Pendimethalin 30.0 33.0 40.0 40.0 40.0 40.0 33.0
    Imazaquin 5.0
    Na+ cresol- 4.7
    formaldehyde
    condensate
    Na+ cresol- 4.2 4.2
    formaldehyde
    sulphonated
    condensate
    Triethanolamine salt of 3.4
    polyarylarylethox-ylate
    phosphate
    Na+ lignosulfonate 4.0 4.8
    Acetic acid to pH 7.4 *
    Polycarboxylate 3.0
    derivative
    Urea 13.3
    Precipitated silica 0.75
    Xanthum gum 0.1 0.1 0.1 0.1 0.1 0.2 0.16
    Formaldehyde 38% 0.25 0.25 0.25 0.25 0.25 0.5 0.4
    solution
    Siliconic antifoam 0.5 0.1 0.5 0.9 0.3 1.0 0.3
    Ethylene glycol 8.0 8.0 8.0 5.0
    Ethylene
    oxide/propylene oxide
    condensate
    Water^ QS QS QS QS QS QS QS

Claims (12)

What is claimed is:
1. A process for the preparation of a stable aqueous suspension concentrate composition which comprises mixing a molten pendimethalin stream having a temperature of about 57° to 75° C. with an aqueous stream containing coformulants plus seed crystals of orange pendimethalin said aqueous stream having a temperature of about −3° C. to 5° C.
2. The process according to claim 1, wherein said seed crystals are present at about 16% to 24%.
3. The process according to claim 1 wherein said coformulants are selected from the group consisting of a surfactant; an antifreeze agent; an antifoam agent; a suspending agent; a thickener; a preservative; a water-soluble pesticide; and a mixture thereof.
4. The process according to claim 3 wherein said surfactant is selected from the group consisting of an ethylene oxide/propylene oxide condensate; an alkylaryl- or arylarylethoxylate; a lignosulfonate; a cresol-formaldehyde condensate or a sulfonate thereof; a naphthalene-formaldehyde condensate or a sulfonate thereof; a polycarboxylate or a derivative thereof; and a mixture thereof.
5. The process according to claim 3 wherein the surfactant is selected from the group consisting of an alkylarylethoxylate; a triethanolamine salt or a potassium salt of polyarylarylethoxylate phosphate; a polyarylarylpolyoxyethylene phosphoric acid; a sodium cresol-formaldehyde condensate; a sodium salt of a sulfonated cresol-formaldehyde condensate; and a mixture thereof.
6. The process according to claim 3 wherein the antifreeze agent is selected from the group consisting of ethylene glycol; propylene glycol; glycerine; urea; and a mixture thereof.
7. The process according to claim 3 wherein the thickener is selected from the group consisting of clay; precipitated silica; polyvinyl alcohol; polyvinylpyrrolidone; polyacrylamide; and a mixture thereof.
8. The process according to claim 3 wherein the preservative is selected from the group consisting of a 38% formaldehyde solution; methyl or propyl parahydroxybenzoate; 2-bromo-2-nitropropane-1,3-diol; sodium benzoate; glutaraldehyde; o-phenylphenol; benzisothiazolinone; methyl or ethyl 4-isothiazolin-3-one; pentachlorophenol; 2,4-dichlorobenzyl alcohol; and a mixture thereof.
9. The process according to claim 8 wherein the preservative is a 38% formaldehyde solution.
10. The process according to claim 3 wherein the water-soluble pesticide is a water-soluble herbicide.
11. The process according to claim 10 wherein said herbicide is selected from the group consisting of a quaternary salt of an amino phosphonic or phosphinic acid; a substituted phenoxy or benzoic acid salt; an imidazolinone; and a mixture thereof.
12. The process according to claim 11 wherein said herbicide is selected from the group consisting of glyphosate; glufosinate; 2,4-D; MCPA; dicamba; imazaquin; imazethapyr; imazapic; imazamox; imazapyr; and a mixture thereof.
US09/938,371 2000-08-25 2001-08-24 Continuous process for the preparation of a stable herbicidal aqueous suspension concentrate composition Expired - Fee Related US6617280B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US09/938,371 US6617280B2 (en) 2000-08-25 2001-08-24 Continuous process for the preparation of a stable herbicidal aqueous suspension concentrate composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US22831600P 2000-08-25 2000-08-25
US09/938,371 US6617280B2 (en) 2000-08-25 2001-08-24 Continuous process for the preparation of a stable herbicidal aqueous suspension concentrate composition

Publications (2)

Publication Number Publication Date
US20020128154A1 true US20020128154A1 (en) 2002-09-12
US6617280B2 US6617280B2 (en) 2003-09-09

Family

ID=22856665

Family Applications (1)

Application Number Title Priority Date Filing Date
US09/938,371 Expired - Fee Related US6617280B2 (en) 2000-08-25 2001-08-24 Continuous process for the preparation of a stable herbicidal aqueous suspension concentrate composition

Country Status (18)

Country Link
US (1) US6617280B2 (en)
EP (1) EP1313366B1 (en)
AR (1) AR030485A1 (en)
AT (1) ATE274300T1 (en)
AU (1) AU2001289832A1 (en)
BG (1) BG66154B1 (en)
CZ (1) CZ295651B6 (en)
DE (1) DE60105174T2 (en)
DK (1) DK1313366T3 (en)
ES (1) ES2225604T3 (en)
HU (1) HUP0300776A2 (en)
IL (2) IL154303A0 (en)
PT (1) PT1313366E (en)
RU (1) RU2003107843A (en)
SK (1) SK286830B6 (en)
TR (1) TR200402441T4 (en)
WO (1) WO2002015690A1 (en)
ZA (1) ZA200302273B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120128750A1 (en) * 2009-07-14 2012-05-24 Basf Se Process for preparing an aqueous suspension of an organic pesticide compound
JP2015040191A (en) * 2013-08-22 2015-03-02 竹本油脂株式会社 Aqueous suspended agrochemical composition

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK1622447T3 (en) 2003-04-14 2010-11-08 Basf Se Aqueous liquid concentrate composition of pendimethalin
AU2009305426B2 (en) * 2008-10-14 2014-12-11 Basf Se Crystalline complexes of pendimethalin and metazachlor
US8420574B2 (en) * 2009-04-20 2013-04-16 Valent Biosciences Corporation Plant growth enhancement with combinations of PESA and herbicides
US10492490B2 (en) * 2015-03-06 2019-12-03 Board Of Trustees Of Michigan State University Adjuvant compositions and related methods for reducing herbicide volatility
CN110699418B (en) * 2019-11-14 2023-06-06 浙江星博生物科技股份有限公司 Detection method based on GC-MS sperm count for non-diagnostic purpose

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3337964A1 (en) * 1983-10-19 1985-05-02 Hoechst Ag, 6230 Frankfurt METHOD FOR PRODUCING PLANT PROTECTIVE DISPERSIONS
US4871392A (en) 1986-05-23 1989-10-03 American Cyanamid Company Aqueous suspension concentrate compositions of pendimethalin
US5624884A (en) * 1986-05-23 1997-04-29 American Cyanamid Company Aqueous suspension concentrate compositions of pendimethalin
DE3916465A1 (en) * 1989-05-20 1990-11-22 Bayer Ag PRODUCTION OF SPHERICAL DISPERSIONS BY CRYSTALLIZATION OF EMULSIONS
FR2670085B1 (en) * 1990-12-10 1996-12-13 Rhone Poulenc Chimie PHYTOSANITARY SUSPENSIONS.

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120128750A1 (en) * 2009-07-14 2012-05-24 Basf Se Process for preparing an aqueous suspension of an organic pesticide compound
US8618022B2 (en) * 2009-07-14 2013-12-31 Basf Se Process for preparing an aqueous suspension of an organic pesticide compound
AU2010272571B2 (en) * 2009-07-14 2015-05-28 Basf Se A process for preparing an aqueous suspension of an organic pesticide compound
EP2453739B2 (en) 2009-07-14 2023-03-01 Basf Se A process for preparing an aqueous suspension of an organic pesticide compound
JP2015040191A (en) * 2013-08-22 2015-03-02 竹本油脂株式会社 Aqueous suspended agrochemical composition

Also Published As

Publication number Publication date
CZ2003862A3 (en) 2003-06-18
WO2002015690A1 (en) 2002-02-28
EP1313366A1 (en) 2003-05-28
BG107567A (en) 2004-08-31
AU2001289832A1 (en) 2002-03-04
EP1313366B1 (en) 2004-08-25
DK1313366T3 (en) 2004-10-04
IL154303A (en) 2007-06-03
DE60105174D1 (en) 2004-09-30
CZ295651B6 (en) 2005-09-14
PL361388A1 (en) 2004-10-04
ZA200302273B (en) 2004-07-15
ATE274300T1 (en) 2004-09-15
TR200402441T4 (en) 2004-12-21
US6617280B2 (en) 2003-09-09
RU2003107843A (en) 2004-07-27
DE60105174T2 (en) 2005-01-13
AR030485A1 (en) 2003-08-20
SK3512003A3 (en) 2003-09-11
HUP0300776A2 (en) 2005-11-28
BG66154B1 (en) 2011-09-30
SK286830B6 (en) 2009-06-05
ES2225604T3 (en) 2005-03-16
PT1313366E (en) 2004-10-29
IL154303A0 (en) 2003-09-17

Similar Documents

Publication Publication Date Title
JP2894608B2 (en) Aqueous suspension concentrate composition of pendimethalin
US4875929A (en) Aqueous suspension concentrate compositions
EP0404201B1 (en) Aqueous suspension concentrate compositions
JPH08501320A (en) Agricultural preparations
US6617280B2 (en) Continuous process for the preparation of a stable herbicidal aqueous suspension concentrate composition
PL188690B1 (en) Oily suspension concentrates
US20150099637A1 (en) New method to improve the performance of herbicide formulations
US5679619A (en) Aqueous suspension concentrate compositions of pendimethalin
US5624884A (en) Aqueous suspension concentrate compositions of pendimethalin
JP2024059827A (en) Pesticide Composition
JPH0419202B2 (en)
PL203503B1 (en) A method of producing a herbicide in the form of a stable aqueous suspension concentrate
AU594774B2 (en) Aqueous suspension concentrate compositions of pendimethalin
SK281366B6 (en) Aqueous suspension concentrate pesticidal compositions and method of preparing thereof
JPH03123707A (en) Herbicide composition

Legal Events

Date Code Title Description
AS Assignment

Owner name: BASF AKTIENGESELLSCHAFT, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:FAFCHAMPS, JEAN-PAUL;VILLANUEVA, JEAN-MICHEL;REEL/FRAME:012662/0630;SIGNING DATES FROM 20011023 TO 20011105

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362

FP Lapsed due to failure to pay maintenance fee

Effective date: 20150909